End-stage renal failure, reflux nephropathy and Feingold's syndrome

Pediatric Nephrology

Volumn 23, Issue 1, 2008, Pages 159-161

  Aslam, Mona ^a   Bokhoven, Hans ^b   Taylor, Christopher Mark ^a  

^a BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

End stage renal failure; Feingold's syndrome; Urinary tract abnormality

Indexed keywords

AZATHIOPRINE; CYCLOSPORIN; PREDNISOLONE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLEPHAROPHIMOSIS; CASE REPORT; CLINICAL FEATURE; DUODENUM ATRESIA; EXON; FACE DYSMORPHIA; FEINGOLD SYNDROME; FEMALE; GESTATIONAL AGE; GROWTH RETARDATION; HUMAN; IMAGING SYSTEM; IMMUNOSUPPRESSIVE TREATMENT; KIDNEY DYSPLASIA; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; NONSENSE MUTATION; PERITONEAL DIALYSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; PTOSIS; REFLUX NEPHROPATHY; STOP CODON; SYNDACTYLY;

ABNORMALITIES, MULTIPLE; CHILD; FEMALE; HUMANS; KIDNEY; KIDNEY FAILURE, CHRONIC; MICROCEPHALY; NUCLEAR PROTEINS; ONCOGENE PROTEINS; SYNDROME; VESICO-URETERAL REFLUX;

EID: 37049006747     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-007-0602-3     Document Type: Article

References (10)

1. Celli J, van Beusekom E, Hennekam RC, Gallardo ME, Smeets DF, de Cordoba SR, Innis JW, Frydman M, Konig R, Kingston H, Tolmie J, Govaerts LC, van Bokhoven H, Brunner HG (2000) Familial syndromic esophageal atresia maps to 2p23-p24. Am J Hum Genet 66:436-444
2. van Bokhoven H, Celli J, van Reeuwijk J, Rinne T, Glaudemans B, van Beusekom E, Rieu P, Newbury-Ecob RA, Chiang C, Brunner HG (2005) MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome. Nat Genet 37:465-467
3. Charron J, Malynn BA, Fisher P, Stewart V, Jeannotte L, Goff SP, Robertson EJ, Alt FW (1992) Embryonic lethality in mice homozygous for a targeted disruption of the N-myc gene. Genes Dev 6:2248-2257
4. Sawai S, Shimono A, Hanaoka K, Kondoh H (1991) Embryonic lethality resulting from disruption of both N-myc alleles in mouse zygotes. New Biol 3:861-869
5. Stanton BR, Perkins AS, Tessarollo L, Sassoon DA, Parada LF (1992) Loss of N-myc function results in embryonic lethality and failure of the epithelial component of the embryo to develop. Genes Dev 6:2235-2247
6. Knoepfler PS, Cheng PF, Eisenman RN (2002) N-myc is essential during neurogenesis for the rapid expansion of progenitor cell populations and the inhibition of neuronal differentiation. Genes Dev 16:699-712
7. Celli J, van Bokhoven H, Brunner HG (2003) Feingold syndrome: Clinical review and genetic mapping. Am J Hum Genet 122:294-300
8. Frydman M, Katz M, Cabot SG, Soen G, Kauschansky A, Sirota L (1997) MODED: Microcephaly-oculo-digito-esophageal-duodenal syndrome. Am J Med Genet 71:251-257
9. Piersall LD, Dowton SB, McAlister WH, Waggoner DJ (2000) Vertebral anomalies in a new family with ODED syndrome. Clin Genet 57:444-448
10. Büttiker V, Wojtulewicz J, Wilson M (2000) Imperforate anus in Feingold syndrome. Am J Med Genet 92:166-169